Syringaresinol-4---d-glucoside alters lipid and glucose metabolism in HepG2 cells and C2C12 myotubes.
10.1016/j.apsb.2017.04.008
- Author:
Shuai WANG
1
;
Chongming WU
1
;
Xin LI
1
;
Yue ZHOU
1
;
Quanyang ZHANG
1
;
Fuchao MA
1
;
Jianhe WEI
1
;
Xiaopo ZHANG
2
;
Peng GUO
1
Author Information
1. Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100094, China.
2. School of Pharmaceutical Science, Hainan Medical University, Haikou 571101, China.
- Publication Type:Journal Article
- Keywords:
C2C12;
Glucose consumption;
HepG2;
Insulin resistance;
Lipid accumulation;
Oil red O;
Syringaresinol-4-O-β-d-glucoside
- From:
Acta Pharmaceutica Sinica B
2017;7(4):453-460
- CountryChina
- Language:English
-
Abstract:
Syringaresinol-4---d-glucoside (SSG), a furofuran-type lignan, was found to modulate lipid and glucose metabolism through an activity screen of lipid accumulation and glucose consumption, and was therefore considered as a promising candidate for the prevention and treatment of metabolic disorder, especially in lipid and glucose metabolic homeostasis. In this study, the effects of SSG on lipogenesis and glucose consumption in HepG2 cells and C2C12 myotubes were further investigated. Treatment with SSG significantly inhibited lipid accumulation by oil red O staining and reduced the intracellular contents of total lipid, cholesterol and triglyceride in HepG2 cells. No effect was observed on cell viability in the MTT assay at concentrations of 0.1-10 μmol/L. SSG also increased glucose consumption by HepG2 cells and glucose uptake by C2C12 myotubes. Furthermore, real-time quantitative PCR revealed that the beneficial effects were associated with the down-regulation of sterol regulatory element-binding proteins-1c, -2 (), fatty acid synthase (), acetyl CoA carboxylase () and hydroxyl methylglutaryl CoA reductase (), and up-regulation of peroxisome proliferator-activated receptors alpha and gamma (and). SSG also significantly elevated transcription activity oftested by luciferase assay. These results suggest that SSG is an effective regulator of lipogenesis and glucose consumption and might be a candidate for further research in the prevention and treatment of lipid and glucose metabolic diseases.
